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Items where Author is "Garbusow, Maria"

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Group by: Date | Item Type | Refereed
Jump to: 2014
Number of items: 3.

2014

Schott, Björn H. and Assmann, Anne and Schmierer, Phöbe and Soch, Joram and Erk, Susanne and Garbusow, Maria and Mohnke, Sebastian and Pohland, Lydia and Romanczuk-Seiferth, Nina and Barman, Adrian and Wustenberg, Torsten and Haddad, Linda and Grimm, Oliver and Witt, Stephanie H. and Richter, Sylvia and Klein, Marieke and Schutze, Hartmut and Muhleisen, Thomas W. and Cichon, Sven and Rietschel, Marcella and Noethen, Markus M. and Tost, H. and Gundelfinger, Eckart D. and Duzel, Emrah and Heinz, Andreas and Meyer-Lindenberg, Andreas and Seidenbecher, Constanze I. and Walter, Henrik . (2014) Epistatic interaction of genetic depression risk variants in the human subgenual cingulate cortex during memory encoding. Translational Psychiatry, 4. e372.

Mohnke, Sebastian and Erk, Susanne and Schnell, Knut and Schütz, Claudia and Romanczuk-Seiferth, Nina and Grimm, Oliver and Haddad, Leila and Pohland, Lydia and Garbusow, Maria and Schmitgen, Mike M. and Kirsch, Peter and Esslinger, Christine and Rietschel, Marcella and Witt, Stephanie H. and Nöthen, Markus M. and Cichon, Sven and Mattheisen, Manuel and Mühleisen, Thomas and Jensen, Jimmy and Schott, Björn H. and Maier, Wolfgang and Heinz, Andreas and Meyer-Lindenberg, Andreas and Walter, Henrik . (2014) Further evidence for the impact of a genome-wide-supported psychosis risk variant in ZNF804A on the Theory of Mind Network. Neuropsychopharmacology, 39 (5). pp. 1196-1205.

Erk, Susanne and Meyer-Lindenberg, Andreas and Schmierer, Phöbe and Mohnke, Sebastian and Grimm, Oliver and Garbusow, Maria and Haddad, Leila and Poehland, Lydia and Muhleisen, Thomas W. and Witt, Stephanie H. and Tost, Heike and Kirsch, Peter and Romanczuk-Seiferth, Nina and Schott, Björn H. and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella and Heinz, Andreas and Walter, Henrik . (2014) Hippocampal and frontolimbic function as intermediate phenotype for psychosis: evidence from healthy relatives and a common risk variant in CACNA1C. Biological Psychiatry, 76 (6). pp. 466-475.

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